Mutagenetix > Incidental Mutation

Incidental Mutation 'R2036:Ppp2r2c'

224613

Institutional Source

Beutler Lab

Gene Symbol

Ppp2r2c

Ensembl Gene

ENSMUSG00000029120

Gene Name

protein phosphatase 2, regulatory subunit B, gamma

Synonyms

6330548O06Rik, IMYPNO1, PR52

MMRRC Submission

040043-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.537) question?

Stock #

R2036 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

37025857-37112422 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 37109748 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 369 (T369I)

Ref Sequence

ENSEMBL: ENSMUSP00000031003 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031003]

AlphaFold

Q8BG02

Predicted Effect

possibly damaging
Transcript: ENSMUST00000031003
AA Change: T369I

PolyPhen 2 Score 0.840 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000031003
Gene: ENSMUSG00000029120
AA Change: T369I

Domain	Start	End	E-Value	Type
WD40	13	52	1.99e0	SMART
WD40	79	119	2.38e1	SMART
WD40	161	200	1.11e0	SMART
WD40	211	251	5.7e1	SMART
WD40	270	308	4.11e1	SMART
Blast:WD40	312	366	1e-24	BLAST
WD40	402	439	3.07e1	SMART

Meta Mutation Damage Score

0.1821

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.8%

Validation Efficiency

100% (58/58)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a gamma isoform of the regulatory subunit B55 subfamily. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930415H17Rik	C	T	11: 99,576,358 (GRCm39)	C3Y	unknown	Het
Abr	G	T	11: 76,343,176 (GRCm39)	T547K	probably benign	Het
Akr1c21	T	C	13: 4,626,305 (GRCm39)	Y110H	probably damaging	Het
Ankar	T	A	1: 72,705,689 (GRCm39)	K556*	probably null	Het
Anks1b	T	C	10: 90,805,715 (GRCm39)	V431A	probably damaging	Het
Ap5b1	T	C	19: 5,618,897 (GRCm39)	S106P	possibly damaging	Het
Arhgap17	T	C	7: 122,917,717 (GRCm39)	N156D	possibly damaging	Het
Arhgap35	T	C	7: 16,297,058 (GRCm39)	E669G	probably damaging	Het
Arhgap44	T	C	11: 64,932,318 (GRCm39)	M201V	possibly damaging	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
Atg4c	C	T	4: 99,106,376 (GRCm39)	T112M	possibly damaging	Het
Bcl11a	A	T	11: 24,114,087 (GRCm39)	N477Y	possibly damaging	Het
Brinp3	A	T	1: 146,577,579 (GRCm39)	I205F	possibly damaging	Het
Capza2	T	C	6: 17,660,777 (GRCm39)	F159S	probably damaging	Het
Cd40	T	C	2: 164,904,221 (GRCm39)	C61R	probably benign	Het
Cdc25c	G	C	18: 34,871,292 (GRCm39)	L275V	probably damaging	Het
Cdh23	A	G	10: 60,301,822 (GRCm39)	I415T	possibly damaging	Het
Clnk	A	T	5: 38,910,143 (GRCm39)		probably null	Het
Ctcfl	C	T	2: 172,943,778 (GRCm39)	R524Q	possibly damaging	Het
Cyb5r4	T	G	9: 86,924,932 (GRCm39)		probably benign	Het
Ddb1	T	A	19: 10,588,186 (GRCm39)		probably benign	Het
Ddx51	C	A	5: 110,804,491 (GRCm39)	Q526K	probably benign	Het
Dennd6a	A	T	14: 26,329,274 (GRCm39)	Q56L	probably damaging	Het
Dhdds	T	C	4: 133,698,410 (GRCm39)	E142G	probably damaging	Het
Dnai1	A	G	4: 41,632,225 (GRCm39)	H553R	probably damaging	Het
Fryl	T	C	5: 73,179,887 (GRCm39)	N2908S	probably benign	Het
Fryl	C	A	5: 73,265,305 (GRCm39)		probably null	Het
Fut9	A	G	4: 25,620,322 (GRCm39)	I164T	probably damaging	Het
Gba2	G	A	4: 43,568,118 (GRCm39)		probably benign	Het
Gm11627	C	T	11: 102,467,580 (GRCm39)	V33I	unknown	Het
Helz2	T	A	2: 180,879,272 (GRCm39)	H782L	probably benign	Het
Kcnmb3	A	G	3: 32,526,531 (GRCm39)	V220A	probably damaging	Het
Kif20a	T	C	18: 34,761,515 (GRCm39)	S303P	possibly damaging	Het
Kif22	A	T	7: 126,630,126 (GRCm39)	V470E	possibly damaging	Het
Majin	C	T	19: 6,263,342 (GRCm39)	T132M	probably benign	Het
Mboat7	A	G	7: 3,688,671 (GRCm39)		probably null	Het
Mkrn2	C	A	6: 115,588,875 (GRCm39)	P206Q	probably benign	Het
Mphosph9	G	A	5: 124,442,274 (GRCm39)	T358M	probably damaging	Het
Nkd1	A	G	8: 89,318,305 (GRCm39)	D210G	probably damaging	Het
Or4c110	C	T	2: 88,831,976 (GRCm39)	V219I	probably damaging	Het
Or4k41	T	A	2: 111,279,971 (GRCm39)	L162Q	possibly damaging	Het
Or5ae2	G	T	7: 84,505,566 (GRCm39)		probably benign	Het
Or5b95	G	C	19: 12,658,165 (GRCm39)	G231A	probably damaging	Het
Or5p69	T	A	7: 107,966,947 (GRCm39)	N83K	probably benign	Het
Or6c35	G	A	10: 129,169,541 (GRCm39)	D264N	probably benign	Het
Or9s15	A	T	1: 92,524,328 (GRCm39)	E29V	probably benign	Het
Pi4ka	A	G	16: 17,120,976 (GRCm39)	Y63H	probably damaging	Het
Plekha1	A	G	7: 130,503,922 (GRCm39)	R210G	probably damaging	Het
Relch	A	G	1: 105,670,979 (GRCm39)	D1029G	probably damaging	Het
Rmnd1	T	C	10: 4,357,884 (GRCm39)	D12G	probably damaging	Het
Rtn2	A	G	7: 19,027,664 (GRCm39)	K120E	probably damaging	Het
Sh3tc1	A	G	5: 35,873,508 (GRCm39)	S30P	probably benign	Het
Tln2	T	C	9: 67,179,986 (GRCm39)	E795G	possibly damaging	Het
Tmprss11d	T	A	5: 86,457,128 (GRCm39)	Y177F	probably damaging	Het
Trrap	C	A	5: 144,765,372 (GRCm39)	D2529E	probably benign	Het
Vmn2r58	A	G	7: 41,513,417 (GRCm39)	Y409H	probably benign	Het
Wdr72	T	A	9: 74,058,876 (GRCm39)	V323D	probably damaging	Het

Other mutations in Ppp2r2c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01319:Ppp2r2c	APN	5	37,104,465 (GRCm39)	missense	possibly damaging	0.82
IGL01583:Ppp2r2c	APN	5	37,026,166 (GRCm39)	start codon destroyed	probably null	0.99
IGL01662:Ppp2r2c	APN	5	37,083,744 (GRCm39)	missense	probably damaging	1.00
IGL01674:Ppp2r2c	APN	5	37,097,570 (GRCm39)	missense	possibly damaging	0.63
IGL02027:Ppp2r2c	APN	5	37,109,816 (GRCm39)	missense	probably damaging	0.99
IGL03118:Ppp2r2c	APN	5	37,083,660 (GRCm39)	missense	probably damaging	1.00
R0034:Ppp2r2c	UTSW	5	37,084,883 (GRCm39)	missense	probably benign	0.02
R4877:Ppp2r2c	UTSW	5	37,026,214 (GRCm39)	missense	probably damaging	0.98
R4980:Ppp2r2c	UTSW	5	37,109,732 (GRCm39)	missense	probably benign	0.01
R5838:Ppp2r2c	UTSW	5	37,097,531 (GRCm39)	missense	probably benign	0.14
R6291:Ppp2r2c	UTSW	5	37,097,468 (GRCm39)	missense	possibly damaging	0.95
R6940:Ppp2r2c	UTSW	5	37,084,875 (GRCm39)	missense	probably damaging	0.98
R7405:Ppp2r2c	UTSW	5	37,104,486 (GRCm39)	missense	possibly damaging	0.71
R7695:Ppp2r2c	UTSW	5	37,104,526 (GRCm39)	missense	probably damaging	1.00
R7967:Ppp2r2c	UTSW	5	37,097,450 (GRCm39)	missense	possibly damaging	0.88
R8307:Ppp2r2c	UTSW	5	37,104,430 (GRCm39)	missense	probably damaging	1.00
R9643:Ppp2r2c	UTSW	5	37,080,383 (GRCm39)	missense	probably damaging	0.99
R9715:Ppp2r2c	UTSW	5	37,097,488 (GRCm39)	missense	possibly damaging	0.92
X0013:Ppp2r2c	UTSW	5	37,083,669 (GRCm39)	missense	probably damaging	1.00
Z1176:Ppp2r2c	UTSW	5	37,088,621 (GRCm39)	missense	probably benign	0.09

Predicted Primers

PCR Primer
(F):5'- AATAGCCTGCTCCATGCCTTAC -3'
(R):5'- TGATATTCTCAGCTGGGTGCC -3'

Sequencing Primer
(F):5'- TTACTAGACAAAGCCCCTGGTTAGG -3'
(R):5'- CAGGCCGTGTGCAGGATC -3'

Posted On

2014-08-25